Job Summary: Support a $700M API facility capital project as a Project Engineer / Equipment Package Lead within a GMP-regulated pharmaceutical manufacturing environment. Lead equipment packages through design, procurement, and delivery while coordinating with vendors, site stakeholders, and external engineering partners.
Numbers & Facts
Location
Boulder, CO
Description
Job Summary:
Support a $700M API facility capital project as a Project Engineer / Equipment Package Lead within a GMP-regulated pharmaceutical manufacturing environment
Lead equipment packages through design, procurement, and delivery while coordinating with vendors, site stakeholders, and external engineering partners
Drive package engineering activities, resolve technical issues, and ensure alignment with project schedules and facility requirements
Work in a fast-paced clean room manufacturing environment with evolving specifications and cross-functional collaboration
Roles & Responsibilities:
Lead assigned equipment packages from design through procurement and delivery
Review vendor submittals, technical drawings, and engineering documentation
Provide technical comments and support approval workflows for vendor deliverables
Coordinate with external design houses to ensure package scope and deliverables meet project requirements
Gather and clarify process, facility, utility, and site requirements where specifications are incomplete or evolving
Track package milestones, procurement schedules, and key project deliverables
Support technical issue resolution across vendors, engineering teams, and site stakeholders
Collaborate with process, facilities, utilities, and operations teams to close technical and project gaps
Maintain alignment with GMP and clean room facility standards
Experience:
5+ years of project engineering experience supporting large CAPEX projects in API pharmaceutical manufacturing environments
Experience managing equipment packages, vendor coordination, and technical submittal reviews
Experience working with solid waste supply systems
Familiarity with GMP-regulated manufacturing facilities and clean room environments
Experience working with large design houses and external engineering partners
Proficiency in Microsoft Office applications
Exposure to equipment turnover, startup, or CQV activities preferred
Peptide or GLP-1 manufacturing experience preferred
Familiarity with AutoCAD and Primavera is a plus
Education:
Bachelor's degree in Engineering or related technical discipline preferred